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FIGURE 3. A, binding of GST-xBTEB1[DBD] to regions of the proximal X. laevis TrβA promoter in vitro. We used EMSA to test the ability of radioinert DNA fragments (1.89 μM/reaction) corresponding to different regions of the proximal TrβA promoter (generated by PCR; see Fig. 2 and supplemental Table 1) to displace GST-xBTEB1[DBD] binding to the 32P-BTE probe. mBTE, mutated BTE. B, binding of GST-xBTEB1[DBD] to GC-rich regions of the proximal TrβA promoter. We used EMSA to test whether GST-xBTEB1[DBD] could bind to short 32P-labeled oligonucleotides encompassing one or two GC boxes in the TrβA promoter. The numbering of the GC boxes included in each oligonucleotide probe is based on that given in Fig. 2 and Table 4. In each case homologous, radioinert competitors (1.89 μM) were used to displace binding.

Image published in: Bagamasbad P et al. (2008)

Copyright © 2008. Image reproduced with permission of the publisher and the copyright holder. This is an Open Access article distributed under the terms of the Creative Commons Attribution License.

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